CH461794A - Gegen die Einwirkung von Hitze, Sauerstoff und Licht stabilisierte Formmasse - Google Patents
Gegen die Einwirkung von Hitze, Sauerstoff und Licht stabilisierte FormmasseInfo
- Publication number
- CH461794A CH461794A CH768462A CH768462A CH461794A CH 461794 A CH461794 A CH 461794A CH 768462 A CH768462 A CH 768462A CH 768462 A CH768462 A CH 768462A CH 461794 A CH461794 A CH 461794A
- Authority
- CH
- Switzerland
- Prior art keywords
- heat
- oxygen
- light
- threads
- molding compound
- Prior art date
Links
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 title claims description 5
- 238000000465 moulding Methods 0.000 title claims description 5
- 229910052760 oxygen Inorganic materials 0.000 title claims description 5
- 239000001301 oxygen Substances 0.000 title claims description 5
- 150000001875 compounds Chemical class 0.000 title claims description 4
- 230000000694 effects Effects 0.000 title description 3
- 239000002262 Schiff base Substances 0.000 claims description 5
- 150000004753 Schiff bases Chemical class 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 4
- 125000005521 carbonamide group Chemical group 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 230000000087 stabilizing effect Effects 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 description 9
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 6
- 239000004952 Polyamide Substances 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 229920002647 polyamide Polymers 0.000 description 4
- -1 3, 4-methylenedioxy Chemical group 0.000 description 3
- UFFRSDWQMJYQNE-UHFFFAOYSA-N 6-azaniumylhexylazanium;hexanedioate Chemical compound [NH3+]CCCCCC[NH3+].[O-]C(=O)CCCCC([O-])=O UFFRSDWQMJYQNE-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 229920002396 Polyurea Polymers 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- OCPBTGFXVLONGM-UHFFFAOYSA-N 1-(1,3-benzodioxol-5-yl)-n-phenylmethanimine Chemical compound C1=C2OCOC2=CC=C1C=NC1=CC=CC=C1 OCPBTGFXVLONGM-UHFFFAOYSA-N 0.000 description 2
- RWKMGMPVESDCBV-UHFFFAOYSA-N 6-(1,3-benzodioxol-5-ylmethylideneamino)hexan-1-amine Chemical compound C1OC2=CC=C(C=NCCCCCCN)C=C2O1 RWKMGMPVESDCBV-UHFFFAOYSA-N 0.000 description 2
- UTGQNNCQYDRXCH-UHFFFAOYSA-N N,N'-diphenyl-1,4-phenylenediamine Chemical compound C=1C=C(NC=2C=CC=CC=2)C=CC=1NC1=CC=CC=C1 UTGQNNCQYDRXCH-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- JREWGBQIWACPOA-UHFFFAOYSA-N ethyl 4-amino-6-(1,3-benzodioxol-5-ylmethylidene)cyclohexa-2,4-diene-1-carboxylate Chemical compound C(C)OC(C1C(C=C(C=C1)N)=CC1=CC2=C(C=C1)OCO2)=O JREWGBQIWACPOA-UHFFFAOYSA-N 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- CKVFMHUYNFWPAY-UHFFFAOYSA-N 1-n-benzyl-4-n-phenylbenzene-1,4-diamine Chemical compound C=1C=CC=CC=1CNC(C=C1)=CC=C1NC1=CC=CC=C1 CKVFMHUYNFWPAY-UHFFFAOYSA-N 0.000 description 1
- PWXIKGAMKWRXHD-UHFFFAOYSA-N 3-butylaziridin-2-one Chemical compound CCCCC1NC1=O PWXIKGAMKWRXHD-UHFFFAOYSA-N 0.000 description 1
- 229940044174 4-phenylenediamine Drugs 0.000 description 1
- QLHGKUQCPKIEIW-UHFFFAOYSA-N C1OC=2C=C(C=NCCN)C=CC=2O1 Chemical compound C1OC=2C=C(C=NCCN)C=CC=2O1 QLHGKUQCPKIEIW-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- YDLSUFFXJYEVHW-UHFFFAOYSA-N azonan-2-one Chemical compound O=C1CCCCCCCN1 YDLSUFFXJYEVHW-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- AAYWZUWKFAOYGC-UHFFFAOYSA-N n-(1,3-benzodioxol-5-ylmethylideneamino)-n-phenylaniline Chemical compound C1=C2OCOC2=CC=C1C=NN(C=1C=CC=CC=1)C1=CC=CC=C1 AAYWZUWKFAOYGC-UHFFFAOYSA-N 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- XUWHAWMETYGRKB-UHFFFAOYSA-N piperidin-2-one Chemical compound O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyamides (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB63266A DE1169130B (de) | 1961-07-14 | 1961-07-14 | Verfahren zum Verbessern der Bestaendigkeit von lineare Carbonamidgruppen enthaltenden Polykondensaten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH461794A true CH461794A (de) | 1968-08-31 |
Family
ID=6973918
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH768462A CH461794A (de) | 1961-07-14 | 1962-06-26 | Gegen die Einwirkung von Hitze, Sauerstoff und Licht stabilisierte Formmasse |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3321436A (en)van) |
| BE (1) | BE620256A (en)van) |
| CH (1) | CH461794A (en)van) |
| DE (1) | DE1169130B (en)van) |
| GB (1) | GB1005808A (en)van) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2356728A1 (de) * | 1973-11-14 | 1975-05-15 | Huels Chemische Werke Ag | Gelstippenarmes polylaurinlactam |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2426766A (en) * | 1941-09-27 | 1947-09-02 | Du Pont | Stabilization of organic substances |
| GB826262A (en) * | 1956-11-07 | 1959-12-31 | Harold Newby | Improvements in the stabilisation of polymers |
| US2951832A (en) * | 1958-09-26 | 1960-09-06 | Du Pont | Fluoroelastomers |
| US3115466A (en) * | 1960-05-05 | 1963-12-24 | Ethyl Corp | Synergistic antioxidants |
| US3113880A (en) * | 1961-01-04 | 1963-12-10 | Du Pont | Chemical compounds, polymeric compositions and shaped articles thereof |
| US3216969A (en) * | 1961-10-27 | 1965-11-09 | Universal Oil Prod Co | Polymers stabilized with o-hydroxybenzalaminodiphenylamines or metal coordination complexes thereof |
-
0
- BE BE620256D patent/BE620256A/xx unknown
-
1961
- 1961-07-14 DE DEB63266A patent/DE1169130B/de active Pending
-
1962
- 1962-06-26 CH CH768462A patent/CH461794A/de unknown
- 1962-07-10 GB GB26420/62A patent/GB1005808A/en not_active Expired
- 1962-07-11 US US209261A patent/US3321436A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| BE620256A (en)van) | |
| DE1169130B (de) | 1964-04-30 |
| GB1005808A (en) | 1965-09-29 |
| US3321436A (en) | 1967-05-23 |
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